Canonical Allele Identifier: CA344001662

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059352G>C (hg19) ; chr1:g.197090222G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090222G>C , CM000663.2:g.197090222G>C	GRCh38
NC_000001.10:g.197059352G>C , CM000663.1:g.197059352G>C	GRCh37
NC_000001.9:g.195325975G>C	NCBI36
NG_015867.1:g.61473C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3090C>G
ENST00000367409.9:c.9803C>G MANE Select	ENSP00000356379.4:p.Ala3268Gly
ENST00000680265.1:c.10025C>G	ENSP00000505384.1:p.Ala3342Gly
ENST00000680710.1:c.9779C>G	ENSP00000506676.1:p.Ala3260Gly
ENST00000294732.11:c.5048C>G	ENSP00000294732.7:p.Ala1683Gly
ENST00000367408.5:c.2798C>G	ENSP00000356378.1:p.Ala933Gly
ENST00000367409.8:c.9803C>G	ENSP00000356379.4:p.Ala3268Gly
ENST00000612785.1:c.3761C>G	ENSP00000479244.1:p.Ala1254Gly
NM_001206846.1:c.5048C>G	NP_001193775.1:p.Ala1683Gly
NM_018136.4:c.9803C>G	NP_060606.3:p.Ala3268Gly
NM_018136.5:c.9803C>G MANE Select	NP_060606.3:p.Ala3268Gly
NM_001206846.2:c.5048C>G	NP_001193775.1:p.Ala1683Gly